(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(2,4-difluorophenyl)propanoic acid
≥95%
- Product Code: 37422
CAS:
1217820-78-4
| Molecular Weight: | 423.41 g./mol | Molecular Formula: | C₂₄H₁₉F₂NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07371997 | |
| Melting Point: | Boiling Point: | 618.5±55.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily utilized in the field of peptide synthesis, where it serves as a protected amino acid derivative. Its structure includes a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is commonly used to shield the amino group during the synthesis process. The presence of the 2,4-difluorophenyl group in the molecule makes it particularly useful in the development of peptides with specific binding properties or biological activities. It is often employed in the production of peptide-based drugs, where precise control over the sequence and structure of the peptide is crucial. Additionally, its application extends to research in medicinal chemistry, where it is used to study the interactions of peptides with various biological targets.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,374.00 |
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| 0.250 | 10-20 days | ฿8,748.00 |
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(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(2,4-difluorophenyl)propanoic acid
This compound is primarily utilized in the field of peptide synthesis, where it serves as a protected amino acid derivative. Its structure includes a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is commonly used to shield the amino group during the synthesis process. The presence of the 2,4-difluorophenyl group in the molecule makes it particularly useful in the development of peptides with specific binding properties or biological activities. It is often employed in the production of peptide-based drugs, where precise control over the sequence and structure of the peptide is crucial. Additionally, its application extends to research in medicinal chemistry, where it is used to study the interactions of peptides with various biological targets.
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